Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts5 |
G |
T |
16: 85,665,083 (GRCm39) |
S627Y |
probably damaging |
Het |
Allc |
G |
A |
12: 28,610,010 (GRCm39) |
R196C |
probably damaging |
Het |
Ccdc65 |
A |
C |
15: 98,618,568 (GRCm39) |
E241A |
probably benign |
Het |
Dclk3 |
T |
C |
9: 111,317,741 (GRCm39) |
|
probably benign |
Het |
Fzd4 |
T |
C |
7: 89,056,505 (GRCm39) |
V184A |
probably benign |
Het |
Gfap |
T |
A |
11: 102,784,083 (GRCm39) |
|
probably null |
Het |
Gpr149 |
A |
G |
3: 62,511,366 (GRCm39) |
V211A |
probably benign |
Het |
Gprc6a |
A |
G |
10: 51,491,355 (GRCm39) |
I623T |
probably damaging |
Het |
Gucy2c |
T |
C |
6: 136,696,665 (GRCm39) |
T687A |
probably benign |
Het |
Kcnc4 |
T |
G |
3: 107,355,243 (GRCm39) |
M402L |
possibly damaging |
Het |
Ktn1 |
T |
C |
14: 47,928,391 (GRCm39) |
L584S |
probably damaging |
Het |
Mrgprb2 |
C |
T |
7: 48,202,650 (GRCm39) |
S25N |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,417,875 (GRCm39) |
V3607E |
probably benign |
Het |
Or4c58 |
C |
A |
2: 89,674,913 (GRCm39) |
V135L |
probably benign |
Het |
Or6c3b |
T |
C |
10: 129,527,147 (GRCm39) |
I254M |
probably damaging |
Het |
Otx2 |
A |
G |
14: 48,898,781 (GRCm39) |
I75T |
probably damaging |
Het |
Pabpc4l |
T |
C |
3: 46,400,972 (GRCm39) |
D224G |
probably damaging |
Het |
Peg3 |
A |
T |
7: 6,710,648 (GRCm39) |
C1525S |
probably damaging |
Het |
Polq |
A |
T |
16: 36,865,156 (GRCm39) |
L669F |
probably damaging |
Het |
Prss40 |
A |
C |
1: 34,597,182 (GRCm39) |
V122G |
probably damaging |
Het |
Rims2 |
A |
G |
15: 39,326,009 (GRCm39) |
|
probably null |
Het |
Rrp12 |
A |
T |
19: 41,860,232 (GRCm39) |
M997K |
possibly damaging |
Het |
Sbno2 |
G |
A |
10: 79,902,735 (GRCm39) |
R414W |
probably damaging |
Het |
Scn1a |
T |
C |
2: 66,148,362 (GRCm39) |
D41G |
probably benign |
Het |
Serpinb1c |
A |
T |
13: 33,066,044 (GRCm39) |
D300E |
probably damaging |
Het |
Timeless |
G |
A |
10: 128,087,924 (GRCm39) |
D1165N |
probably damaging |
Het |
Tnpo1 |
T |
G |
13: 99,024,981 (GRCm39) |
K66N |
probably damaging |
Het |
Trappc11 |
A |
T |
8: 47,963,912 (GRCm39) |
N629K |
possibly damaging |
Het |
Ubr4 |
T |
A |
4: 139,179,989 (GRCm39) |
L255M |
probably damaging |
Het |
Vmn1r10 |
T |
A |
6: 57,091,042 (GRCm39) |
Y211* |
probably null |
Het |
Vmn2r76 |
T |
G |
7: 85,879,034 (GRCm39) |
N422T |
probably benign |
Het |
Xylt1 |
C |
A |
7: 117,192,940 (GRCm39) |
N415K |
probably damaging |
Het |
Zfp786 |
A |
T |
6: 47,798,458 (GRCm39) |
V160E |
possibly damaging |
Het |
|
Other mutations in 1700113H08Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01688:1700113H08Rik
|
APN |
10 |
87,000,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01764:1700113H08Rik
|
APN |
10 |
86,909,910 (GRCm39) |
start codon destroyed |
probably benign |
0.02 |
IGL02173:1700113H08Rik
|
APN |
10 |
87,061,754 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02756:1700113H08Rik
|
APN |
10 |
87,000,970 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03202:1700113H08Rik
|
APN |
10 |
86,909,911 (GRCm39) |
start codon destroyed |
probably null |
0.35 |
R0255:1700113H08Rik
|
UTSW |
10 |
87,061,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R0409:1700113H08Rik
|
UTSW |
10 |
87,061,816 (GRCm39) |
missense |
probably damaging |
0.98 |
R0744:1700113H08Rik
|
UTSW |
10 |
87,000,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R0833:1700113H08Rik
|
UTSW |
10 |
87,000,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R1163:1700113H08Rik
|
UTSW |
10 |
86,957,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R2128:1700113H08Rik
|
UTSW |
10 |
87,066,066 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2129:1700113H08Rik
|
UTSW |
10 |
87,066,066 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4108:1700113H08Rik
|
UTSW |
10 |
87,061,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:1700113H08Rik
|
UTSW |
10 |
87,061,808 (GRCm39) |
missense |
probably benign |
0.00 |
R6345:1700113H08Rik
|
UTSW |
10 |
87,061,913 (GRCm39) |
missense |
probably benign |
0.43 |
R6372:1700113H08Rik
|
UTSW |
10 |
87,066,088 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6710:1700113H08Rik
|
UTSW |
10 |
87,061,923 (GRCm39) |
missense |
probably benign |
0.00 |
R6971:1700113H08Rik
|
UTSW |
10 |
87,000,903 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7055:1700113H08Rik
|
UTSW |
10 |
87,062,083 (GRCm39) |
missense |
probably damaging |
0.99 |
R7713:1700113H08Rik
|
UTSW |
10 |
87,066,173 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7808:1700113H08Rik
|
UTSW |
10 |
86,957,297 (GRCm39) |
missense |
probably benign |
0.33 |
R7838:1700113H08Rik
|
UTSW |
10 |
87,042,061 (GRCm39) |
splice site |
probably null |
|
R8293:1700113H08Rik
|
UTSW |
10 |
87,061,864 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9041:1700113H08Rik
|
UTSW |
10 |
87,062,054 (GRCm39) |
missense |
probably benign |
0.03 |
R9351:1700113H08Rik
|
UTSW |
10 |
87,066,068 (GRCm39) |
missense |
probably benign |
0.27 |
|